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Enrolling By InvitationNCT07008469

Global Open-Label Extension Study of Del-desiran for the Treatment of DM1

A Global Phase 3 Open-Label Extension Study to Assess the Long-Term Safety, Tolerability, and Efficacy of Intravenous AOC 1001 for the Treatment of Myotonic Dystrophy Type 1

Status
Enrolling By Invitation
Phase
Phase 3
Study type
Interventional
Enrollment
230 (estimated)
Sponsor
Avidity Biosciences, Inc. · Industry
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

A Global Phase 3 Open-Label Extension Study to Assess the Long-Term Safety, Tolerability, and Efficacy of Intravenous Delpacibart Etedesiran (abbreviated del-desiran, formerly AOC 1001) for the Treatment of Myotonic Dystrophy Type 1

Detailed description

The study consists of a Screening Period of up to either 4-weeks or 8-weeks depending on the prior parent trial, and up to a 4-year Treatment Period. The anticipated duration is 50 months and 2 weeks (4 years and 2.5 months). Participants will receive an intravenous infusion of del-desiran at the clinical study site every 8 weeks for a total of 7 doses per year. The final dose will occur at Year 4, Visit 7, followed by a final assessment 8 weeks after the last dose. An additional subgroup of de novo participants will also be included in a Fixed-Dose PK cohort. An Independent Data Monitoring Committee (IDMC) comprised of members independent and external to the Sponsor will review safety, tolerability, and efficacy (as needed) data of this study at regular intervals.

Conditions

Interventions

TypeNameDescription
DRUGDel-desiran (AOC 1001)Del-desiran will be administered by intravenous (IV) infusion.

Timeline

Start date
2025-07-25
Primary completion
2030-08-01
Completion
2030-10-01
First posted
2025-06-06
Last updated
2026-02-03

Locations

20 sites across 5 countries: United States, Canada, Italy, Japan, Netherlands

Regulatory

Source: ClinicalTrials.gov record NCT07008469. Inclusion in this directory is not an endorsement.